Canonical Allele Identifier: CA1998714675

Gene: ACAT1

Linked Data

• dbSNP Id: rs2077415740

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.108134168_108134169insTATTAT , CM000673.2:g.108134168_108134169insTATTAT	GRCh38
NC_000011.9:g.108004895_108004896insTATTAT , CM000673.1:g.108004895_108004896insTATTAT	GRCh37
NC_000011.8:g.107510105_107510106insTATTAT	NCBI36
NG_009888.1:g.17638_17639insTATTAT
NG_009888.2:g.22464_22465insTATTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265838.9:c.239-53_239-52insTATTAT MANE Select	ENSP00000265838.4:n.239-53_239-52insTATTAT
ENST00000671707.1:n.334-53_334-52insTATTAT
ENST00000672008.1:c.239-53_239-52insTATTAT	ENSP00000500499.1:n.239-53_239-52insTATTAT
ENST00000672031.1:c.239-53_239-52insTATTAT	ENSP00000500463.1:n.239-53_239-52insTATTAT
ENST00000672284.1:c.-32-53_-32-52insTATTAT	ENSP00000500444.1:n.-32-53_-32-52insTATTAT
ENST00000672354.1:c.239-53_239-52insTATTAT	ENSP00000500490.1:n.239-53_239-52insTATTAT
ENST00000672367.1:c.73-4730_73-4729insTATTAT	ENSP00000500209.1:n.73-4730_73-4729insTATTAT
ENST00000672580.1:c.239-53_239-52insTATTAT	ENSP00000500366.1:n.239-53_239-52insTATTAT
ENST00000672907.1:c.120+2214_120+2215insTATTAT	ENSP00000500928.1:n.120+2214_120+2215insTATTAT
ENST00000673000.1:n.327-53_327-52insTATTAT
ENST00000673531.1:c.-32-53_-32-52insTATTAT	ENSP00000500163.1:n.-32-53_-32-52insTATTAT
ENST00000265838.8:c.239-53_239-52insTATTAT	ENSP00000265838.4:n.239-53_239-52insTATTAT
ENST00000299355.10:c.239-53_239-52insTATTAT	ENSP00000299355.6:n.239-53_239-52insTATTAT
ENST00000524833.5:n.279-53_279-52insTATTAT
ENST00000527942.5:c.-32-53_-32-52insTATTAT	ENSP00000433568.1:n.-32-53_-32-52insTATTAT
ENST00000528370.1:c.45-53_45-52insTATTAT
ENST00000531813.5:c.239-53_239-52insTATTAT	ENSP00000435965.1:n.239-53_239-52insTATTAT
ENST00000531853.5:n.503-53_503-52insTATTAT
NM_000019.3:c.239-53_239-52insTATTAT	NP_000010.1:n.239-53_239-52insTATTAT
XM_006718834.2:c.-32-53_-32-52insTATTAT	XP_006718897.1:n.-32-53_-32-52insTATTAT
XM_006718835.2:c.-32-53_-32-52insTATTAT	XP_006718898.1:n.-32-53_-32-52insTATTAT
XM_006718835.3:c.-32-53_-32-52insTATTAT	XP_006718898.1:n.-32-53_-32-52insTATTAT
XM_017017681.1:c.-32-53_-32-52insTATTAT	XP_016873170.1:n.-32-53_-32-52insTATTAT
XM_017017682.2:c.-39-53_-39-52insTATTAT	XP_016873171.1:n.-39-53_-39-52insTATTAT
XM_017017683.2:c.-39-53_-39-52insTATTAT	XP_016873172.1:n.-39-53_-39-52insTATTAT
XM_024448511.1:c.-32-53_-32-52insTATTAT	XP_024304279.1:n.-32-53_-32-52insTATTAT
XM_024448512.1:c.-32-53_-32-52insTATTAT	XP_024304280.1:n.-32-53_-32-52insTATTAT
XM_024448513.1:c.-32-53_-32-52insTATTAT	XP_024304281.1:n.-32-53_-32-52insTATTAT
XM_024448514.1:c.-32-53_-32-52insTATTAT	XP_024304282.1:n.-32-53_-32-52insTATTAT
XM_024448515.1:c.-32-53_-32-52insTATTAT	XP_024304283.1:n.-32-53_-32-52insTATTAT
NM_000019.4:c.239-53_239-52insTATTAT MANE Select	NP_000010.1:n.239-53_239-52insTATTAT
NM_001386677.1:c.239-53_239-52insTATTAT	NP_001373606.1:n.239-53_239-52insTATTAT
NM_001386678.1:c.120+2214_120+2215insTATTAT	NP_001373607.1:n.120+2214_120+2215insTATTAT
NM_001386679.1:c.-39-53_-39-52insTATTAT	NP_001373608.1:n.-39-53_-39-52insTATTAT
NM_001386681.1:c.-32-53_-32-52insTATTAT	NP_001373610.1:n.-32-53_-32-52insTATTAT
NM_001386682.1:c.-32-53_-32-52insTATTAT	NP_001373611.1:n.-32-53_-32-52insTATTAT
NM_001386685.1:c.-32-53_-32-52insTATTAT	NP_001373614.1:n.-32-53_-32-52insTATTAT
NM_001386686.1:c.-32-53_-32-52insTATTAT	NP_001373615.1:n.-32-53_-32-52insTATTAT
NM_001386687.1:c.-32-53_-32-52insTATTAT	NP_001373616.1:n.-32-53_-32-52insTATTAT
NM_001386688.1:c.-32-53_-32-52insTATTAT	NP_001373617.1:n.-32-53_-32-52insTATTAT
NM_001386689.1:c.-32-53_-32-52insTATTAT	NP_001373618.1:n.-32-53_-32-52insTATTAT
NM_001386690.1:c.-32-53_-32-52insTATTAT	NP_001373619.1:n.-32-53_-32-52insTATTAT
NM_001386691.1:c.-32-53_-32-52insTATTAT	NP_001373620.1:n.-32-53_-32-52insTATTAT
NR_170162.1:n.279-53_279-52insTATTAT
NR_170163.1:n.373-53_373-52insTATTAT